Serum TSH level as predictor of Graves' disease recurrence following antithyroid drug withdrawal: A systematic review

PLoS One. 2021 Jan 29;16(1):e0245978. doi: 10.1371/journal.pone.0245978. eCollection 2021.

Abstract

Graves' disease (GD) has a high recurrence rate despite various and adequate treatment. Numerous studies have been performed to identify the predictor of disease recurrence. This report aims to investigate the role of thyroid stimulating hormone (TSH) level as a thyrotropin in predicting the recurrence of Graves' disease within 1 to 2 years following antithyroid drug (ATD) withdrawal. Literature searching was conducted on PubMed, Scopus, Cochrane, Proquest, EBSCO in August 2019 and Google Scholar in October 2020. The study criteria include the study that evaluates TSH level 4 weeks following ATD withdrawal, with subjects ≥18 years old who are retrospectively or prospectively followed up after 1 to 2 years following ATD withdrawal. Four eligible studies were selected based on inclusion/exclusion criteria, all of which measured TSH level at 4 weeks following ATD withdrawal. All studies had 1 to 2 years follow up. One study was an RCT, two studies were done in prospective cohort and another in retrospective cohort. All studies had comparable validity and applicability. Three out of four studies suggested that low TSH level measured 4 weeks following treatment withdrawal was associated with higher risk of disease recurrence. In conclusion, low TSH level obtained 4 weeks after ATD withdrawal was associated with higher rate of recurrence rate in GD.

Publication types

  • Research Support, Non-U.S. Gov't
  • Systematic Review

MeSH terms

  • Antithyroid Agents / therapeutic use*
  • Graves Disease / blood
  • Graves Disease / diagnosis*
  • Graves Disease / drug therapy
  • Humans
  • Recurrence
  • Thyrotropin / blood*
  • Withholding Treatment

Substances

  • Antithyroid Agents
  • Thyrotropin

Grants and funding

This study was funded by Indonesian Ministry of Education and Research, Grant numbers: NKB-1539/UN2.R3.1/HKP.05.00/2019.